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Italian Journal of Neurological Sciences|April 1, 1994
Toxic effect of intraventricular interferon-alpha in subacute sclerosing panencephalitisC Cianchetti, A L Fratta, F Muntoni, et al.Neuromuscular Disorders : NMD|May 1, 1997
Gene conversion at the SMN locus in autosomal recessive spinal muscular atrophy does not predict a mild phenotypeK Talbot, N R Rodrigues, J Ignatius, et al.Neuromuscular Disorders : NMD|November 26, 1998
A severe clinical and pathological variant of central core disease with possible autosomal recessive inheritanceA Y Manzur, C A Sewry, J Ziprin, et al.Brain & Development|May 1, 1996
Clinical and EEG findings in eleven patients affected by mitochondrial encephalomyopathy with MERRF-MELAS overlapG Serra, R Piccinnu, M Tondi, et al.Neuromuscular Disorders : NMD|January 1, 1997
Diagnosis of X-linked Emery-Dreifuss muscular dystrophy by protein analysis of leucocytes and skin with monoclonal antibodiesS Manilal, C A Sewry, N Man, et al.Neuropediatrics|January 4, 2005
Bone mineral density in a paediatric spinal muscular atrophy populationM Kinali, L M Banks, E Mercuri, et al.Journal of Inherited Metabolic Disease|August 11, 2004
OCTN2 mutation (R254X) found in Saudi Arabian kindred: recurrent mutation or ancient founder mutation?A-M Lamhonwah, R Onizuka, S E Olpin, et al.Human Genetics|October 30, 1999
Is there selection in favour of heterozygotes in families with merosin-deficient congenital muscular dystrophy?M D'Alessandro, I Naom, A Ferlini, et al.American Journal of Human Genetics|July 31, 1998
A novel Alu-like element rearranged in the dystrophin gene causes a splicing mutation in a family with X-linked dilated cardiomyopathyA Ferlini, N Galié, L Merlini, et al.QRB. Quality Review Bulletin|May 1, 1978
Blurred vision: problems of auditing elective surgery, as seen in an audit of lens extraction for cataractD N CohenPageof 166